Glioblastoma cells block radiation-induced programmed cell death of endothelial cells

被引:44
|
作者
Brown, CK
Khodarev, NN
Yu, JQ
Moo-Young, T
Labay, E
Darga, TE
Posner, MC
Weichselbaum, RR
Mauceri, HJ [1 ]
机构
[1] Univ Chicago, Dept Radiat & Cellular Oncol, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Surg, Chicago, IL 60637 USA
来源
FEBS LETTERS | 2004年 / 565卷 / 1-3期
关键词
co-culture; endothelial cell survival; DNA repair and checkpoint gene; VEGF; DNA array;
D O I
10.1016/j.febslet.2004.03.099
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We demonstrate that human umbilical vein endothelial cells (HUVEC) grown in co-culture (CC) with U87 Glioblastoma. cells transfected with green fluorescent protein (GFP-U87) exhibit resistance to radiation-mediated apoptosis. cDNA macroarray analysis reveals increases in the accumulation of RNAs for HUVEC genes encoding cell adhesion molecules, growth factor-related proteins, and cell cycle regulatory/DNA repair proteins. An increase in protein expression of integrin alpha(v), integrin beta(1), MAPK(p42), Rad51, DNA-PKCS, and ataxia telangiectasia gene (ATM) was detected in HUVEC grown in CC with GFP-U87 cells compared with HUVEC grown in mono-culture. Treatment with anti-VEGF antibody decreases the expression of integrin alpha(v), integrin beta(1), DNA-PKCS and ATM with a corresponding increase in ionizing radiation (IR)-induced apoptosis. These data support the concept that endothelial cells growing in the tumor microenvironment may develop resistance to cytotoxic therapies due to the up-regulation by tumor cells of endothelial cells genes associated with survival. (C) 2004 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:167 / 170
页数:4
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